Targeted gene deletions for polysaccharide slime formers

ABSTRACT

Sphingomonas  strains have extracellular polysaccharide (e.g., gellan, diutan) that is firmly attached to the cell surface. This attachment may limit polysaccharide production by impairing uptake of nutrients into the cell or due to limited sites for polysaccharide biosynthesis on the cell surface. Two genes for polysaccharide biosynthesis, designated gelM and gelN in gellan-producing strains and dpsM and dpsN in diutan-producing strains, have been inactivated by deletion mutations and shown to produce polysaccharide that is not firmly attached to the cell surface, i.e., slime form. Another gene for polysaccharide biosynthesis, designated gelI in gellan producing strains, was inactivated by insertion mutation and also shown to produce the slime phenotype. The homologous gene dpsi in the diutan producing strain should also be involved in the attachment of the polysaccharide to the cell surface. The slime characteristic was demonstrated by the ability of the cells to be centrifuged and the lack of cell clumping as seen under the microscope or in diluted suspensions. The diutan slime mutants had somewhat increased productivity and the recovered diutan product had significantly improved rheology. Gellan slime mutants had lower broth viscosity which facilitates mixing during fermentation; however, the recovered gellan product had lower gel strength than the gellan produced from a capsular strain. A deletion in a gene gelR, which encodes a protein with homology to surface proteins and outer membrane proteins and weak homology to proteins with polysaccharide degradation activity, was shown to restore higher gel strength to the slime form of gellan, and to produce gellan of higher gel strength than that of the capsular gellan producing strains.

This application claims the benefit of U.S. Provisional Application No. 60/649,559, filed Feb. 4, 2005.

TECHNICAL FIELD OF THE INVENTION

This invention is related to the area of sphingan polysaccharide production. In particular, it relates to site-directed genetic methods for improving sphingan-producing strains.

BACKGROUND OF THE INVENTION

Sphingomonas strains, such as ATCC 53159 and ATCC 31461, produce copious amounts of capsular polysaccharide. While under some conditions polysaccharide may be released from the cell [5, 6], during growth with abundant carbon source as in fermentation, the polysaccharide is firmly attached to the cell surface. Attempts to increase productivity of fermentations for diutan and gellan may be limited by the capsular nature of the polysaccharide, which may impair uptake of nutrients. Also, if there are a limited number of sites for biosynthesis of the polysaccharide, there may be a maximum amount of polysaccharide that can be produced by each cell. The polysaccharide gellan has been observed to be involved in cell clumping since mutants that do not make any polysaccharide grow uniformly in suspension [3]. These cell clumps may interfere with techniques such as determination of cell number by optical density, centrifugation of cells, e.g., for isolation of DNA or protein, and separation or lysis of cells for polysaccharide purification.

The mechanism of attachment and the genes involved in attachment of polysaccharide to the cell surface in Sphingomonads have not been previously determined. Induced mutants of Sphingomonas strains ATCC 31461, ATCC 31555, ATCC 31554, and ATCC 21423 that produce polysaccharide in a slime form have been isolated, but the genes mutated were not determined, and the methods of inducing and selecting the mutants were not disclosed [10]. Genes for biosynthesis of gellan [3, 8], diutan [1] and sphingan S-88 [9] have been isolated. The functions of many of these genes were assigned by biochemical tests or by homology to genes of known functions in databases such as GenBank. For example, genes have been identified that are involved in assembly of the tetrasaccharide repeat unit [7, 8], and in synthesis of the precursor dTDP-L-rhamnose [3, 9]. It would be expected that genes affecting only attachment of polysaccharide to the cell surface would still have the polysaccharide producing phenotype (i.e., mucoid colonies on solid media and viscous broth).

A cluster of 18 genes for gellan biosynthesis spanning 21 kb was described, in addition to four genes for gellan synthesis not in the cluster Harding N. E., Y. N. Patel, and R. Coleman, 2004. Organization of genes required for gellan polysaccharide biosynthesis in Sphingomonas elodea ATCC 31461. J Ind Microbiol Biotech 31:70-82, reference 3. The DNA sequences were deposited in GenBank in June 2003 (Accession number AY217008). Among the genes in the cluster were gelM, gelN, and gelI. A deletion of most of adjacent genes gelM and gelN was constructed. The gelI gene was inactivated by an insertion. The gelM-gelN deletion strain and the gelI mutant were shown to produce somewhat reduced amounts of gellan and more fluid broths, and the gellan produced was shown to have the same composition as gellan from the wild-type strain. The attachment of the polysaccharide to the cell was not reported

The Sphingomonas elodea gelR, gelS, and gelG genes appear to be in an operon in the same order as in the S-88 sps gene cluster, but not adjacent to the genes in the cluster of 18 genes (reference 3). The GelR protein was somewhat smaller than its S-88 homolog (659 vs. 670 amino acids) with 49% identity, and had homology to surface layer proteins and other membrane proteins. The DNA sequences of gelR, gelS and gelG genes were deposited in GenBank in June 2003 (Accession number AY220099). No mutation in gelR was constructed in this report (reference 3). Yamazaki et al. report that strains with mutations in gene spsR were still mucoid, indicating that they produce polysaccharide, but the polysaccharide was not characterized as to rheology or attachment to the cell ([9] and T. J. Pollock et al. DNA segments and methods for increasing polysaccharide production. U.S. Pat. No. 5,854,034.

Yamazaki described classical mutants of four Sphingomonas strains that produce polysaccharide as slime rather than attached to the cell. U.S. Pat. No. 6,605,461. Yamazaki did not describe how to screen mutagenized cultures for the slime phenotype. Yamazaki did not identify which gene or genes were mutated.

Sa-Correia reviewed work done on isolation of genes for gellan synthesis. Sa-Correia I., A. M. Fialho, P. Videira, L. M. Moreira, A. R. Marques and H. Albano. 2002. Gellan gum biosynthesis in Sphingomonas paucimobilis ATCC 31461: Genes, enzymes and exopolysaccharide production engineering. J Ind Microbiol Biotechnol. 29: 170-176. Sa-Correia described partial sequencing of some genes including urf32 and urf26 (=gelM and gelN of reference 3 above). The complete sequences of these genes were deposited in GenBank in April 2003 (GenBank Accession number AY242074). No function of these genes is reported. In the GenBank submission, genes urf32 and urf26 were merely designated as putative membrane protein and putative exported protein, respectively. No sequence for gelI or gelR was deposited.

Coleman describes the isolation of genes for diutan biosynthesis and investigation of some gene functions. R. Coleman, 2001, Cloning and analysis of Sphingomonas sp. ATCC 53159 polysaccharide genes. Master's Thesis, San Diego State University. The dpsM and dpsN genes, which were designated by Coleman as orf3 and orf4, were described but functions were not indicated.

A cluster of genes for biosynthesis of the S-88 polysaccharide from Sphingomonas strain ATCC 31554 was described. Yamazaki M., L. Thorne, M. Mikolajczak, R. W. Armentrout and T. J. Pollock. 1996. Linkage of genes essential for synthesis of a polysaccharide capsule in Sphingomonas strain S88. J Bacteriol 178: 2676-2687 and U.S. Pat. No. 5,854,034. The functions of genes urf32 and urf26 (homologs of dpsM, gelM and dpsN, gelN), and spsI (homolog of gelI, dpsI) were not described. Gene spsR (homolog of gelR, dpsR) was described as encoding a protein remotely similar to bacterial and fungal polysaccharide lyases The DNA sequences were deposited in GenBank (Accession number U51197).

There is a continuing need in the art to improve methods of making industrially useful sphingans and the properties of the sphingans.

SUMMARY OF THE INVENTION

According to one embodiment of the invention a method is provided of making a bacterium. The bacterium is of the genus Sphingomonas and comprises a mutation in one or more genes selected from the group consisting of genes M, N I or R of the sphingan polysaccharide biosynthetic gene cluster. The M and N genes are also referred to in some publications, e.g., references 8 and 9, as genes urf32, urf26, respectively (for unknown reading frame). A segment of genomic DNA of a first bacterium of the genus Sphingomonas is isolated. The segment comprises all or part of genes M and/or N or I or R of the sphingan polysaccharide biosynthetic gene cluster. A mutation in the segment is induced to form a mutated segment. The mutated segment is introduced into a second bacterium of the genus Sphingomonas. The second bacterium comprises wild-type genes M and/or N, or I, or R of the sphingan polysaccharide biosynthetic gene cluster. A progeny of the second bacterium in which the mutated segment has integrated in the genome and replaced wild-type genes M and/or N or I, or R of the sphingan polysaccharide biosynthetic gene cluster of the second bacterium is isolated. The Sphingomonas bacterium may or may not be S. elodea.

According to another embodiment of the invention another method is provided of making a bacterium of the genus Sphingomonas which comprises a mutation in one or more genes selected from the group consisting of genes M, N, I, and R of the sphingan polysaccharide biosynthetic gene cluster. Two non-contiguous segments of genomic DNA of a first bacterium of the genus Sphingomonas are isolated. The segments flank or include genes M and N of the sphingan polysaccharide biosynthetic gene cluster. Similarly, segments flanking gene I or gene R can be isolated. The two non-contiguous segments are ligated together. The ligated non-contiguous segments are introduced into a second bacterium of the genus Sphingomonas. The second bacterium comprises wild-type genes M and/or N or I or R of a sphingan polysaccharide biosynthetic gene cluster. A progeny of the second bacterium in which the ligated segment has integrated in the genome and replaced wild-type genes M and/or N or I or R of a sphingan polysaccharide biosynthetic gene cluster of the second bacterium is isolated. The Sphingomonas bacterium may or may not be S. elodea.

According to yet another embodiment of the invention a composition is provided. The composition comprises a native gellan polysaccharide with gel strength greater than that of an equivalent weight of native gellan from a capsular strain.

According to yet another embodiment of the invention a composition is provided. The composition comprises a diutan polysaccharide which imparts to a fluid an increased viscosity relative to an equivalent weight of diutan produced by strain ATCC 53159.

According to another embodiment of the invention an isolated and purified bacterium of the genus Sphingomonas is provided. The bacterium comprises a deletion in one or more genes selected from the group consisting of genes M, N, I, and R of the sphingan polysaccharide biosynthetic gene cluster. The bacterium can be cultured in a culture medium under conditions suitable for producing sphingan polysaccharide to produce sphingan polysaccharide in the culture medium. The culture broth of the bacterium can be used directly as a viscosifier or gelling agent, or after precipitation with alcohol. Alternatively, the culture broth can be subjected to a procedure to remove bacteria from the culture broth prior to use as a viscosifier or gelling agent or recovery from the broth. The Sphingomonas bacterium may or may not be S. elodea.

These and other embodiments which will be apparent to those of skill in the art upon reading the specification provide the art with new methods, strains, and compositions for making viscosifiers and gelling agents.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Comparison of gene clusters for polysaccharide biosynthesis in Sphingomonas strains ATCC 31554, ATCC 31461 and ATCC 53159.

FIG. 2. Slime forming characteristics of S60WTC gelM-gelN mutants

FIG. 3. Slime forming characteristics of S60WTC gelN and gelI Mutants

FIG. 4. Sequence of DNA at the site of deletion of dpsN (SEQ ID NO: 19), and amino acid sequence of the fusion peptide (SEQ ID NO: 20).

FIG. 5A-5C. Slime forming characteristics of dpsN mutants

FIG. 6A-6B. Slime forming characteristics of dpsM mutants

DETAILED DESCRIPTION OF THE INVENTION

Genes have been identified that control the attachment of polysaccharide to bacterial cells in two Sphingomonas strains. Deletion of either one or both genes gelM (dpsm) and gelN (dpsN) or inactivation of gelI results in polysaccharide being released into the medium as slime rather than attached to the cell surface as capsular polysaccharide. Formation of slime form of polysaccharide eases handling of bacterial cultures, improves mixing during fermentation, may increase production, and in some cases improves rheology of the polysaccharide. Site directed mutagenesis is advantageous over random mutagenesis and screening for slime-forming mutants for many reasons, including speed and avoidance of unrelated mutations. Inactivation of the gene gelR was found to improve the rheology (gel strength) of the slime form of gellan polysaccharide.

Orthologs of dpsM, dpsN, gelM, gelN, and gelI can be inactivated in any Sphingomonas strain to obtain the slime-forming phenotype. Orthologs of gelR can be inactivated to prevent degradation of the polysaccharide resulting in improved rheology. Suitable Sphingomonads include without limitation those which make rhamsan (ATCC 31961), welan (ATCC 31555), gellan (ATCC 31461), and diutan (ATCC 53159) and strains making polysaccharides S7 (ATCC 21423), S88 (ATCC 31554), S198 (ATCC 31853) and NW11 (ATCC 53272). The ATCC numbers refer to the deposit numbers of the strains at the American Type Culture Collection. These are exemplified by S. elodea ATCC 31461 and Sphingomonas sp. ATCC 53159, but other strains can be used. Suitable Sphingomonads which can be used include Sphingomonas adhaesiva, Sphingomonas aerolata, Sphingomonas alaskensis, Sphingomonas aquatilis, Sphingomonas aromaticivorans, Sphingomonas asaccharolytica, Sphingomonas aurantiaca, Sphingomonas capsulata, Sphingomonas chlorophenolica, Sphingomonas chungbukensis, Sphingomonas cloacae, Sphingomonas echinoides, Sphingomonas elodea, Sphingomonas faeni, Sphingomonas herbicidovorans, Sphingomonas koreensis, Sphingomonas macrogoltabidus, Sphingomonas mali, Sphingomonas melonis, Sphingomonas natatoria, Sphingomonas parapaucimobilis, Sphingomonas paucimobilis, Sphingomonas pituitosa, Sphingomonas pruni, Sphingomonas rosa, Sphingomonas sanguinis, Sphingomonas sp., Sphingomonas stygia, Sphingomonas subarctica, Sphingomonas suberifaciens, Sphingomonas subterranea, Sphingomonas taejonensis, Sphingomonas terrae, Sphingomonas trueperi, Sphingomonas ursincola, Sphingomonas wittichii, Sphingomonas xenophaga, Sphingomonas yabuuchiae, and Sphingomonas yanoikuyae. Orthologs can be identified on the basis of gene location and organization in a sphingan biosynthetic gene cluster, on the basis of overall homology, and/or on the basis of domain homology. Typically the level of overall homology will be greater than 44%, often greater than 55%, 66%, 77%, 88%, or 98% with one of the dpsM, dpsN, gelM, gelN, gelI or gelR genes. An ortholog desirably has homology greater than 80% with at least one of these four genes.

Site directed mutagenesis can be used to make mutations in a desired known target gene or genomic region. This eliminates the trial-and-error nature of random induced mutagenesis or spontaneous mutagenesis. Formation of deletions insures that the mutations will not revert, as is possible with point (substitution) mutations and insertion mutations, for example. Deletions also have the benefit of not employing exogenous DNA, such as drug resistance markers or other environmentally undesirable markers.

An isolated segment of genomic DNA comprising the M and/or N, I or R of the sphingan biosynthetic gene cluster or flanking DNA is DNA that is not connected to genomic DNA to which it is normally attached. Isolated DNA can be obtained by purification from natural sources, by synthesis, or by amplification, as non-limiting examples. The isolated DNA will typically be on a fragment of DNA in vitro, but isolated DNA could also be on a vector, such as a plasmid or transducing phage, which contains the desired portion of the Sphingomonas genome. Flanking DNA is typically from the genomic regions immediately adjacent to the M and/or N, I or R within about 500 bp of the genes, or within about 1-2 kb of the genes.

Any method known in the art can be used to introduce a mutation into an isolated segment comprising all or part of genes M and/or N, I or R of the sphingan biosynthetic gene cluster. A deletion can be introduced using restriction endonucleases, for example, and rejoining formerly non-contiguous nucleotides. A deletion can be formed by amplifying and joining two non-contiguous segments of the genes or two non-contiguous segments of DNA flanking the target gene. An insertion can be made in an isolated segment using endonuclease digestion and ligation. Chemical mutagenesis can be used on an isolated segment of genomic DNA. Any mutagenesis method can be selected and used according to the particular circumstances.

After mutations have been induced, the segment of genomic DNA can be reintroduced into a recipient bacterium. Typically, but not necessarily, the recipient will be of the same species as the donor of the segment. Any method known in the art for introducing exogenous DNA into a bacterium can be used. Suitable methods include without limitation electroporation, conjugation, spheroplast formation, calcium chloride precipitation and transformation, liposomes, and viral transduction. Any nucleic acid introduction method can be selected and used according to the particular circumstances.

If the segment of mutated genomic DNA introduced into the recipient bacterium does not have a means of replicating itself, then it must integrate into a replicon in the recipient bacterium in order to be maintained. Typically such an integration event will integrate the entire incoming plasmid. One can detect a marker on the introduced DNA to identify that the DNA has integrated. In order to detect resolution of the integrate, one can screen or select for loss of a marker on the introduced DNA. Suitable markers for accomplishing this are known in the art, and any can be used as the circumstances dictate. To determine the isolates in which the introduced version of the sphingan genes replaces the wild-type version in the recipient, the size or sequence of the DNA can be determined, for example, by PCR.

As demonstrated below, the slime form of sphingan produced for example by a sphingan biosynthetic gene cluster gene M and/or N, mutant may have improved rheological properties over the form which is attached to bacterial cells. Such improved Theological properties are reflected in the ability of the same weight of material to provide more viscosifying power. Such improvement may be modest, such as at least 5% 10%, 15%, 20% or 25%, or it can be more substantial, with an improvement of at least 30%, 40%, 50%, 60%, 70%, 80%, or 90% relative to the sphingan produced by the capsule-forming parent. Rheologically properties can be measured using any technique which is known in the art. Suitable techniques include without limitation the measurement of Low Shear Rate Viscosity (“LSRV”) in tap water solutions and the measurement of Sea Water Viscosity (“SWV”) in high salt solutions.

The slime form of gellan, produced for example by a gelN mutant in combination with a mutation in the putative lyase gene gelR results in formation of gellan of high gel strength. The gel strength will typically e greater than 1000, whereas the capsular strain typically produces a gellan with gel strength of 700-900 but less than 1000.

Purified bacteria according to the present invention are those which have been microbiologically purified, for example using liquid dilution techniques or streaking on solid media to form single colonies. Standard techniques known in the art of microbiology can be used for this purpose.

Mutants according to the present invention can be cultured and grown using the same or similar techniques as used for the parental strains. Liquid culture properties of the mutants may be improved, permitting increased aeration and mixing. The culture broth of the mutant may also provide more efficient recovery than with the attached form of polysaccharide. In addition, the mutants may also provide a product with improved clarity relative to the attached form of polysaccharide. Bacteria may optionally be removed from the polysaccharide produced by the mutant by filtration, centrifugation, or by sedimentation. The culture broth can be chemically, enzymatically, or thermally (hot or cold) treated before or after bacteria removal, as desired.

The genes from S. elodea ATCC 31461 involved in gellan attachment to the cell surface are gelM and gelN. (FIG. 1; SEQ ID NO: 13) and gelI (FIG. 1, SEQ ID NO: 25). A strain has been constructed that has a deletion of most of genes gelM and gelN, resulting in the slime-forming phenotype. A specific deletion of gelN has also been constructed, and an insertion in gene gelI. Both of these mutations result in the slime-forming phenotype. The coding sequences of gelM and gelN are at nucleotides 501-1382 and 1366-2064, respectively, in SEQ ID NO: 13. The encoded amino acid sequences are shown at SEQ ID NOs: 16 and 15, respectively. The coding sequences of gelI is at nucleotides 501 to 1403, respectively, in SEQ ID NO: 25. The encoded amino acid sequences are shown at SEQ ID NOs: 26 A deletion of gene gelR was found to result in improved gel strength for gellan in the slime form. The coding sequences of gelR is at nucleotides 478 to 2457, respectively, in SEQ ID NO: 27 The encoded amino acid sequences are shown at SEQ ID NOs: 28. The genes from Sphingomonas sp. ATCC 53159 involved in diutan attachment to the cell surface are dpsM and dpsN (FIG. 1; SEQ ID NO: 14), and presumably dpsI based on homology to gelI. Deletions of each of genes dpsM and dpsN have been constructed and both result in the slime-forming phenotype. The coding sequences of dpsM and dpsN are at nucleotides 456-1337 and 1321-2019, respectively, in SEQ ID NO: 14. The encoded amino acid sequences are shown at SEQ ID NOs: 18 and 17, respectively.

It will be apparent to those skilled in the art that the same or similar methods used for gellan synthesis may also be used for diutan synthesis. Thus mutations in genes dpsI and dpsR could readily be constructed The coding sequences of dpsI is at nucleotides 501-1472, respectively, in SEQ ID NO: 29 The encoded amino acid sequences are shown at SEQ ID NOs: 30 The coding sequences of dpsR is at nucleotides 501-2498, respectively, in SEQ ID NO: 31. The encoded amino acid sequences are shown at SEQ ID NOs. 32.

The above disclosure generally describes the present invention. All references disclosed herein are expressly incorporated by reference. A more complete understanding can be obtained by reference to the following specific examples which are provided herein for purposes of illustration only, and are not intended to limit the scope of the invention.

EXAMPLE 1 Production of Gellan Slime-Forming Mutants

For construction of mutants of Sphingomonas elodea a derivative of ATCC 31461 designated S60 wtc¹ was used, which has improved uptake of DNA. This strain can be readily made by one skilled in the art. PCR amplification was used to amplify regions flanking the gelM-gelN genes. See reference 3. The amplified fragments were cloned into the pLO2 vector and introduced into S60 wtc by conjugation to replace the gelM and ge/N genes on the genome with the deletion, by double crossover homologous recombination. Vector pLO2 does not replicate in S60 wtc, so initial selection for kanamycin resistance selects for those colonies in which the plasmid has integrated into the chromosome by homologous recombination. The vector also contains the gene sacB. This gene confers sensitivity to sucrose. Thus selection on sucrose can be used to detect isolates that have lost the plasmid and retain one copy of the deletion or wild-type genes ¹ S. elodea ATCC 31461 has a low efficiency of uptake of DNA, particularly large plasmids (about 10⁻⁷). Spontaneous mutants of ATCC 31461 with increased efficiency of DNA uptake were isolated. It was suspected that those few cells that were successful recipients of a plasmid such as the broad-host-range plasmid pLAFR3 represented mutants in the recipient population with an increased ability to take up this plasmid DNA. To allow loss of the plasmid, three transconjugants containing pLAFR3 were grown under nonselective conditions (i.e., without tetracycline antibiotic) with serial passage for about 30 generations. Three independent plasmid-cured strains (i.e., tetracycline-sensitive derivatives from each of the initial transconjugants) were tested and all three exhibited increased conjugation frequency (4.2×10⁻³, 0.6×10⁻², and 1.5×10⁻²), representing a 10⁵-fold increase compared to the wild-type strain. This increased conjugation frequency was stable and reproducible. One of these strains was designated S60 wtc. See reference 3.

A plasmid containing the gelM-gelN deleted region was introduced into S60 wtc by tri-parental conjugal mating, using pRK2013 to provide transfer functions, and transconjugants selected on YM-Sm (25 ug/ml)-Km (7.5 ug/ml) medium. Streptomycin prevents growth of the E. coli strains. Kanamycin resistant plasmid integrants were isolated. Sucrose sensitivity was used to select for a second recombination event which eliminated the vector. Five isolates were passed two times under non-selective conditions, i.e., without antibiotic. Aliquots were then plated on medium with 8% sucrose. Sucrose resistant colonies were isolated and tested for kanamycin sensitivity. Genomic DNA was isolated and PCR was used to determine which Kms isolates had retained the deletion. An amplified fragment of the expected size for a deletion resulted from the genomic DNA from four strains. These four deletion strains were purified on YM medium. All four strains appeared less mucoid, softer, flatter and darker yellow than the wild type.

EXAMPLE 2 Characterization of gelM-gelN Deletion Strains

The gelM-gelN deletion isolates were evaluated in shake flask fermentations. The ΔgelM-gelN culture broth was fluid and smooth compared to the more solid, viscous S60 wtc broth. Precipitation with isopropyl alcohol produced longer, thicker, fibers from the mutant strains compared to S60 wtc fibers. However, the deletion mutants had 22% reduction in yield of total precipitable material and produced only 30% of the broth viscosity of wild-type. The gellan produced had a normal composition of sugars, and glyceryl and acetyl substituents.

The mutants were evaluated for slime forming characteristics, using several techniques, including microscopic evaluation, cell clumping, cell pellet formation, and hot settling test, as shown in FIG. 2.

The hot settling test consisted of heating the gellan broth in the autoclave for ten minutes to melt the gellan, then transferring the hot broth to a large test tube and incubating overnight at 95° C. (to maintain broth as liquid). With a capsular strain, the cells are attached to the polysaccharide and remain suspended. For slime-formers, the cells are not attached and settle during overnight incubation. The gelM-gelN deletion strains were shown to be slime formers by this test.

For the centrifugation test, the strains were grown overnight in DM2 media containing 1% glucose and centrifuged at maximum speed in the Eppendorf centrifuge. Inactivation of gelM-N genes results in complete loss of attachment of the polysaccharide from the cell surface such that the cells can be pelleted by centrifugation.

By microscopic evaluation, most of the S60 wtcΔgelM-N cells are free and motile, whereas the S60 wtc are in the gum matrix. In cell culture, the S60 wtcΔgelM-N cells grow in suspension whereas S60 wtc cells form clumps.

EXAMPLE 3 Construction of Gellan Slime-Forming Mutants

A deletion was constructed of gelN for gellan biosynthesis. PCR primers were designed to amplify DNA fragments upstream (500 bp) and downstream (401 bp) of the gelN gene [3]. Primers used are shown in Table 1. TABLE 1 Primers for construction of gelN deletion mutant. Primer Sequence Purpose SacI-GelN primer 1 5′ TGGAGCTC-GGTGCTGTGGTTGTTCTT 3′ Amplifies 500 bp upstream (SEQ ID NO: 1) of gelN XbaI-GelN primer 2 5′ GGTCTAGA-GTCAGGCCGGTTGAACAT 3′ (SEQ ID NO: 2) XbaI-GelN primer 3 5′ AGTCTAGA-GCCTGAACGCCGAAAGGG 3′ Amplifies 401 bp (SEQ ID NO: 3) downstream of gelN SphI-GelN primer 4 5′ GTTGCATGC-GGTGATGGTGGAGAATGG 3′ (SEQ ID NO: 4)

Primers SacI-GelNprimer1 and XbaI-GelNprimer2 were used to amplify a 500 bp fragment from the gelM gene as a SacI-XbaI fragment (total 516 bp). Primers XbaI-GelNprimer3 and SphI-GelNprimer4 were used to amplify a 401 bp fragment from the atrD gene as an XbaI-SphI fragment (total 418 bp). Since the end of the gelM gene overlaps the start of the gelN gene by 17 bp, the stop codon of gelM and the start codon of gelN were retained, as well as the natural stop codon of gelN. The PCR fragments were ligated sequentially into the polylinker of plasmid vector pLO2 [4], resulting in clone pLO2-ge/Ndeln#1 carrying the deletion of gelN.

Plasmid pLO2-gelNdeln#1 was then used to transfer the deletion to strain S60 wtc³ by conjugation and homologous recombination. Strain S60 wtc is a strain derived from ATCC 31461 as a spontaneous mutant with increased ability to take up plasmid DNA [2]. A chromosomal integrant was selected by kanamycin resistance. Subsequent growth for approximately 30 generations in the absence of antibiotic allowed for excision of the plasmid. Recombinants that had lost the plasmid were then selected by sucrose (8%) tolerance, due to loss of the plasmid-encoded sacB gene, and then colonies were screened for kanamycin sensitivity. The sacB gene encodes an enzyme levansucrase for synthesis of levan from sucrose. Levan is toxic to the cells. Cells that have lost the sacB gene can grow on sucrose. The sucrose tolerant isolates can be wild-type or deletion. Genomic DNA was prepared from several isolates to identify those isolates that had retained the gelN deletion versus the wild-type gene, as determined by PCR. Isolates with the gelN deletion had softer, more watery colonies compared to the hard colonies of the wild-type gelN+ isolates. ³ See footnote 1 regarding use of mutant with increased ability to take up DNA.

EXAMPLE 4 Characterization of gelN Deletion Mutants

The gelN deletion mutants had similar properties to the gelM-gelN deletion mutants. Cells were readily pelleted by centrifugation. In cell culture, the gelN deletion mutants grew in suspension, whereas the wild-type cells formed clumps. Thus, inactivation of the gelN gene can result in the slime phenotype as shown in FIG. 3.

Five individual isolates of gelN deletion mutants were evaluated in shake flask fermentations. The average yield (total precipitable material, TPM) for the gelN mutants (1.10 g/100 ml) was comparable to that of the S60 wtc control (1.08 g/100 ml). Selected gelN mutants were evaluated in 20L Applikon fermentors using media containing organic and inorganic nitrogen, salts and corn syrup. Gellan polysaccharide was precipitated with isopropyl alcohol, dried and weighed. Average yield of total precipitable material for the mutants was 94% of that of the wild-type control, however the broth viscosity was decreased by about 40%. This decrease in broth viscosity facilitates mixing in the fermentors. TABLE 2 Fermentation characteristics of gelN mutants TPM Broth Viscosity Strain g/L Cp Wild-type 12.80 5500 gelN #1 12.04 3850 gelN #2 12.15 2700 gelN #4 11.80 3400 average 12.00 3317 Viscosity was measured in the Brookfield LVF viscometer using the No.4 spindle at 60 rpm.

EXAMPLE 5 Construction of Mutants Producing Gellan Slime with Improved Quality

The slime mutants of gellan had lower broth viscosity, as described in Example 4, which facilitates mixing in the fermentors. Gellan polysaccharide forms a gel after heating and cooling, and gellan is used in various food applications due to its unique textural and rheological properties. Therefore, the gel strength of the gellan produced by the slime mutants was evaluated. The gel strength is determined by the break or fracture of a prepared gel surface with a plunger.

The gellan fermentation broth was adjusted to pH 4.6 (to prevent deacylation) and pasteurized by heating to about 100° C. for several minutes. Gellan product was precipitated by addition of three times volume of isopropyl alcohol, and the fibers dried at 60° C. for two hours and milled.

A calcium solution was prepared by adding 2 ml of a 0.3 M CaCl₂.2H₂O stock solution to 295 ml of deionized water in a tared 600 ml stainless steel beaker. While stirring the solution at 700 rpm, 3.0 g of gellan product was added and allowed to disperse for 1 to 2 minutes. The beaker was placed into a preheated water bath at 94-95° C. for four minutes, covered and heated for 15 minutes, then stirred for 3 minutes. Solution weight was adjusted to 300 g with heated deionized water, mixed and then left standing at 94-95° C. Solution was transferred into six ring molds (0.5 inch height, 1.375 inch outer diameter, 0.125 inch wall thickness) and covered with a plastic cover plate and allowed to cool at room temperature (20-21° C.) for 20 to 24 hours. The disc was removed from the mold onto a plexiglass plate. Gel strength, or force to break, (recorded in g/cm 2) was determined in a TA-TX2 Texture Analyzer with a Kobe plunger (TA-19) at 1.0 mm/s.

Gellan from the slime mutants had lower gel strength than that from the wild-type capsular stain, as shown in Table 4. This result was in contrast to mutants of ATCC 53159 that produce the slime form of diutan, which had improved rheology as described in Example 11. It was considered possible that the slime form of gellan may be degraded by a gellan lyase enzyme, produced by S. elodea. Therefore, a strain was constructed that has a deletion of a gene, gelR, which produces a protein with homology to polysaccharide degrading proteins, e.g. lyases.

The gelR deletion was constructed in S. elodea strain S60 wtc and strain GBAD-1 (U.S. Patent application No. 20060003051 [11]). PCR primers were designed to amplify DNA fragments upstream (502 bp) and downstream (435 bp) of the gelR gene. PCR primers used are shown in Table 3. TABLE 3 Primers used for construction of gelR deletion Primer Sequence Purpose SacI-GelR primer 1 5′ ACGAGCTCAGATCAGCCGCAACCTCCT 3′ Amplifies 486 bp (Seq ID No :21) upstream of gelR XbaI-GelR primer 2 5′ GCTCTAGA-CGCCGCCATGTTAATCACC 3′ (Seq ID No: 22) XbaI-GelR primer 3 5′ GCTCTAGA-GATGCGTTCCACGCCTGAC 3′ Amplifies 419 bp (Seq ID No: 23) downstream of gelR SphI-GelR primer 4 5′ ATGCATGC-CGATCGCGCTCATCAGGGT 3′ (Seq ID No: 24)

Primers SacI-GelR primer 1 and XbaI-GelR primer 2 were used to amplify a 498 bp fragment upstream of gelR as a SacI-XbaI fragment (total 502 bp). Primers XbaI-GelR primer 3 and SphI-GelR primer 4 were used to amplify a 419 bp fragment downstream of gelR as an XbaI-SphI fragment (total 435 bp). The PCR fragments were digested with restriction enzymes and ligated sequentially into the polylinker of plasmid vector pLO2 [4] resulting in clone pLO2-gelRdeletn #4, carrying the deletion of gelR.

Plasmid pLO2-gelRdeletn #4, which cannot replicate in Sphingomonas, was transferred into S. elodea strains S60 wtc and GBAD-1 by conjugation from E. coli DH5α, using helper plasmid pRK2013 that supplies transfer functions [2]. Chromosomal integrants were selected by kanamycin resistance on YM medium with kanamycin and streptomycin (to counterselect E. coli). Subsequent growth of the Sphingomonas integrants for approximately 30 generations in the absence of antibiotic allowed for the excision of the plasmid. Recombinants that had lost the plasmid were selected by sucrose tolerance due to loss of the plasmid encoded sacB gene, and colonies screened for kanamycin sensitivity. PCR was used to test which isolates had retained the gelR deletion.

The gelN deletion was than transferred into the gelR deletion mutant of the GBAD-1 strain as described above in Example 3. Plasmid pLO2-gelNdeln#1 was used to transfer the gelN deletion into GBADgelR by conjugation and homologous recombination. A chromosomal integrant was selected by kanamycin resistance on YM agar with Km (20 ug/ml) and Sm (25 ug/ml). Subsequent growth in the absence of antibiotic allowed for excision of the plasmid. Recombinants that had lost the plasmid were selected by sucrose tolerance due to loss of the plasmid-encoded sacB gene and then colonies were screened for kanamycin sensitivity.

The gelR deletion mutants exhibited different colony morphology than the wild-type strains. The gelR deletion strains had smaller rough gummy colonies compared to larger smooth gummy colonies with transparent edges for the gelR+ of S60 wtc or GBAD-1. The gelN-gelR deletion mutants had colony morphology similar to the gelN slime mutants.

EXAMPLE 6 Characterization of gelN-gelR Mutants

These strains were evaluated in 20L Applikon fermentors using media containing organic and inorganic nitrogen, salts and corn syrup. Gellan polysaccharide was precipitated with isopropyl alcohol, dried and weighed. Gel strength was determined by the method described in Example 5. The GBAD-1gelNgelR strain produced gellan of higher gel strength than the gellan produced from the gelN slime mutants or the wild-type capsular strains. TABLE 4 Rheological characterization of gellan from mutants Aver TPM Aver. % of Broth Visc Aver Strain Phenotype n = wild-type cP Gel strength S60wtc capsule 3 — 7292 411 GBAD1 capsule 1 91 4600 629 GelN mutants slime 7 93 2900 132 GBAD1gelRgelN slime 3 96 5083 1447

EXAMPLE 7 Construction of gelI Mutant

An insertion mutation in gene gelI was constructed. PCR primers were designed to amplify an internal fragment of the ge/I gene (see reference 3). The amplified fragment was cloned into the pLO2 plasmid vector and introduced into S60 wtc by conjugation, selecting on YM-Sm (25 ug/ml)-Km (7.5 ug/ml) medium. Selection for kanamycin resistance selects for those transconjugants that have the plasmid inserted by homologous recombination into the gelI gene, thus inactivating this gene. The gelI mutant had altered colony morphology, similar to that of the gelM-gelN and the gelN deletion strains, i.e. mucoid but softer colonies.

EXAMPLE 8 Characterization of gelI Mutant Strain

The gelI mutant was evaluated in shake flask fermentation. The mutant had less viscous broth compared to the wild-type strain and about a 20% reduction in yield of total precipitable material. The gellan produced had a normal composition of sugars and glyceryl and acetyl substituents (reference 3).

The gelI mutant was evaluated for slime forming characteristic using several techniques including microscopic evaluation, cell clumping, cell pellet formation and hot settling test as described above. The gelI insertion mutant had similar characteristics to the gelM-gelN and the gelN deletion mutants. Microscopic evaluation showed that the cells were free and motile. In cell culture, the gelI mutants grew in suspension rather than clumps. Cells were readily pelleted from DM2 medium by centrifugation. Cells also settled well in the hot settling test. Thus, the mutation in the gelI gene also results in the slime phenotype as shown in FIG. 3.

EXAMPLE 9 Production of Diutan Slime-Forming Mutants

Sphingomonas sp. ATCC 53159 (S-657) produces a polysaccharide (diutan) with a structure similar to that of gellan (i.e., it has a glucose-glucuronic acid-glucose-rhamnose repeat unit), but with a side chain of two rhamnose residues attached to one glucose residue. Diutan has two acetyl substituents, and lacks glyceryl groups. Diutan is useful as a viscosifier in oilfield and cement applications. Sphingomonas strains produce polysaccharides as capsules firmly bound to the cell surface. The exact mechanism of attachment is not known. The capsule may limit productivity by impairing oxygen uptake. The functionality of the polysaccharide may be hindered by its being attached to the cell rather than free in solution.

Strain Construction:

We constructed deletions of the corresponding genes dpsM and dpsN of Sphingomonas sp. ATCC 53159, which produces diutan (S-657). Each gene was deleted independently and the effect on capsule to slime determined. Briefly, PCR was used to amplify two fragments homologous to DNA flanking the target gene. These fragments were cloned into a narrow-host-range plasmid pLO2 that cannot replicate in Sphingomonas and contains two selective markers, kan^(R) and sacB. Selection for kanamycin resistance selects for cells in which the plasmid has integrated into the chromosome in one of the homologous regions. The kanamycin resistant strain was then grown under nonselective conditions to allow loss of the plasmid by a second recombination. Loss of plasmid was selected by tolerance to sucrose. The sacB gene encodes an enzyme levansucrase for synthesis of levan from sucrose. Levan is toxic to the cells. Cells that have lost the sacB gene can grow on sucrose. The sucrose tolerant isolates can be wild-type or deletion. Presence of the deletion was confirmed by PCR. Mutants were tested for slime or capsule production. No foreign DNA, plasmid, or antibiotic resistance genes remained in the final strain.

Detailed Construction of dpsN and dpsM Deletions Strains

Deletions of dpsM and dpsN were constructed on a plasmid and transferred to the genome of ATCC 53159, using a gene replacement strategy similar to that described for S. elodea deletion mutants [3]. PCR was used to amplify DNA regions flanking the target gene and then the fragments cloned into plasmid pLO2 [4], which was then used to exchange the deletion for the target gene in the chromosome. Primers used for the PCR are shown in Table 5. Restriction sites for cloning (shown in italics) were added to the ends of the primers. TABLE 5 Primers for construction of deletion mutations. Primer Sequence Purpose SacI-DpsN primer 1 5′ TTGAGCTC-GCTGTGGCTGTTCTTCCT 3′ Amplifies 497 bp (SEQ ID NO: 5) upstream of dpsN XbaI-DpsN primer 2 5′ CGTCTAGA-GTCACGCCGGTTGAACAT 3′ (SEQ ID NO: 6) XbaI-DpsN primer 3 5′ TCTCTAGA-CTCGGTCACCAGGTCTGAA 3′ Amplifies 396 bp (SEQ ID NO: 7) downstream of dpsN SphI-DpsN primer 4 5′ CTCGCATGC-CGGTAAAGGTGAAG 3′ (SEQ ID NO: 8) SacI-DpsM primer 1 5′ TTGAGCTC-GATCGGCGTTAAGACTGC 3′ Amplifies 474 bp (SEQ ID NO: 9) upstream of dpsM XbaI-DpsM primer 2 5′ CGTCTAGA-TCATCGCGGTCGCTGCCAT 3′ (SEQ ID NO: 10) XbaI-DpsM primer 3 5′ CCTCTAGA-CGTCGGAGGCATCATGTTC 3′ Amplifies 509 bp (SEQ ID NO: 11) downstream of dpsM SphI-DpsM primer 4 5′ TCGCATGC-TCTGCTGATTGCCGTTCT 3′ (SEQ ID NO: 12)

Deletion constructions were designed to leave the remaining genes for diutan synthesis intact. For the dpsN deletion, primers SacI-DpsNprimer1 and XbaI-DpsNprimer2 were used to amplify a 497 bp fragment from the dpsM gene as a SacI-XbaI fragment (total 513 bp). Primers XbaI-DpsNprimer3 and SphI-DpsNprimer4 were used to amplify a 396 bp fragment from the atrD gene as an XbaI-SphI fragment (total 413 bp). Since the end of the dpsM gene overlaps the start of the dpsN gene by 17 bp, the stop codon of dpsM and the start codon of dpsN were retained, as well as the natural stop codon of dpsN. Thus this construction may result in formation of a small peptide of 13 amino acids, as shown in FIG. 2. The PCR fragments were ligated sequentially into the polylinker of plasmid vector pLO2 [4], resulting in clone pLO2-dpsNdeln#3 carrying the deletion of dpsN.

This plasmid, pLO2-dpsNdeln#3 which cannot replicate in Sphingomonas, was transferred into the Sphingomonas strain ATCC 53159 by conjugation from E. coli DH5α using a helper plasmid pRK2013 that supplies transfer functions [2]. Chromosomal integrants were selected by kanamycin resistance on YM medium with 7.5 ug/ml kanamycin, and 25 ug/ml streptomycin (to counterselect E. coli). Subsequent growth of the Sphingomonas strains for approximately 30 generations in the absence of antibiotic allowed for excision of the plasmid. Recombinants that had lost the plasmid were then selected by sucrose (8%) tolerance, due to loss of the plasmid-encoded sacB gene, and then colonies screened for kanamycin sensitivity. Genomic DNA was prepared from several isolates to identify those isolates that had retained the dpsN deletion versus the wild-type gene, as determined by PCR.

Similarly a deletion of dpsM was constructed. Primers SacI-DpsMprimer1 and XbaI-DpsMprimer2 were used to amplify a 474 bp fragment from the dpsE gene as a SacI-XbaI fragment (total 490 bp). Primers XbaI-DpsMprimer3 and SphI-DpsMprimer 4 were used to amplify a 509 bp fragment from the dpsN gene as a XbaI-SphI fragment (total 525 bp). Since the end of the dpsM gene overlaps the start of the dpsN gene by 17 bp, the stop codon of dpsM and the start codon of dpsN were retained. A stop codon was incorporated within the XbaI cloning site. A 7-amino acid peptide may be formed from the dpsM start site. The PCR fragments were ligated sequentially into the polylinker of plasmid vector pLO2 [4], resulting in clone pLO2-dpsMdeln#1 carrying the deletion of dpsM. This plasmid was transferred by conjugation into ATCC 53159 selecting for kanamycin resistant integrants, followed by growth in the absence of antibiotic and detection of sucrose tolerant, kanamycin sensitive recombinants. Genomic DNA was isolated from selected recombinants and screened by PCR for presence of the deletion.

EXAMPLE 10 Characterization of Diutan Slime-Forming Mutants

Results of several tests showed that both the dpsM and dpsN deletions result in a change from capsule former to slime former, as shown in FIGS. 3 and 4.

-   -   1. Microscopic evaluation of two dpsN deletion mutants (#3 and         #5) and two dpsM deletion mutants (#1 and #5) grown about 16         hours in high carbon fermentation medium indicated that cells         from these mutants did not form the large cell aggregates         characteristic of the Sphingomonas capsular strain, S-657 (FIG.         3 A, and FIG. 4A).     -   2. Wild-type ATCC 53159 cells grown in defined medium (DM2) with         1% glucose for 24 hours and diluted ten-fold formed visible         clumps, where as the dpsM and dpsN slime mutants form uniform         suspensions similar to that of a non-mucoid strain, DPS1 (FIG.         3C for dpsN).     -   3. Centrifugation of 24-hour cultures grown in DM2 medium with         1% glucose showed that the cells from the dpsM and dpsN slime         mutants could be pelleted, whereas those from wild-type ATCC         53159 (S-657) remained attached to the polysaccharide and thus         did not pellet (FIG. 3B and FIG. 4B).

Six independent isolates of dpsN deletion mutants exhibited an average 5.4% increase in total precipitable material compared to the wild-type control, in shake flask fermentations. Selected dpsN and dpsM mutant isolates were evaluated in 20L Applikon fermentors using media containing organic and inorganic nitrogen, salts and different carbon concentrations (3-5%). Polysaccharide was precipitated with isopropyl alcohol, dried and weighed. The dpsN mutants consistently exhibited a slight increase in total precipitable material compared to the wild-type capsular control strain. The dpsM mutants gave more variable and generally lower productivity as shown in Table 6. TABLE 6 Increase in yield of polysaccharide with dps mutants 5% carbon source dpsN #3 n = 3 5.9% dpsN #5 n = 2 3.9% dpsM #1 n = 1 −30.2% dpsM #5 n = 1 9.3% 3% carbon source dpsN #3 n = 2 4.2% dpsM #1 n = 2 −10.1% dpsM #5 n = 4 −2.7%

EXAMPLE 11 Characterization of Diutan Slime-Form Polysaccharide

Rheological properties of diutan recovered from these fermentations by precipitation with isopropyl alcohol was determined as shown in Table 7. Both dpsM and dpsN slime mutations resulted in improved viscosity of diutan. TABLE 7 Rheological properties of diutan from slime mutants % 0.06 s−1 % % Strain SWV3 increase viscosity increase LSRV Increase wild- n = 5 26.7 27,760 2010 type dpsN n = 5 35.3 32% 37,920 37% 3873 93% #3 dpsN n = 2 37.3 40% 41,400 49% 4075 103%  #5 dpsM n = 3 40.5 52% 37,733 36% 3905 94% #1 dpsM n = 5 39.1 46%  39440 42% 3720 85% #5 aver. 42% aver. 41% aver. 94%

It was also observed that fiber quality, e.g., length, was improved with the slime mutants. Since the polysaccharide molecules are free in solution rather than attached to the surface of the cell, the precipitation of these molecules may be facilitated.

Low Shear Rate Viscosity Measurement.

Low shear rate viscosity is the viscosity of a 0.25% solution of diutan at 3 rpm. Standard or synthetic tap water was prepared by dissolving 10 g of NaCl and 1.47 g of CaCl₂.2H₂O in 10 liters of deionized water. 4.5 g of Polyethylene Glycol (PEG) 200 was weighed directly in a 400-ml tall form beaker. A 0.75 g aliquot of diutan product was weighed, and dispersed in the PEG 200 to form a consistent slurry. 299 ml of synthetic tap water was added to the beaker and the mixture stirred at 800±20 rpm for approximately 4 hours. The beaker was removed from the stirring bench and placed in a 25° C. water bath and allowed to stand for 30 min. The viscosity was measured using a Brookfield LV Viscometer with the No. 2 spindle at 3 rpm.

Seawater Viscosity Measurement.

Seawater viscosity was determined using the following procedure. Seawater solution was prepared by dissolving 41.95 g of sea salt (ASTM D-1141-52, from Lake Products Co., Inc. Maryland Heights, Mo.) per 980 g deionized water, with pH adjusted to 8.2 with HCl or NaOH as needed. 307 g of seawater solution was transferred to a mixing cup; 0.86 g of diutan product was slowly added over 15-30 seconds to the mixing cup and allowed to mix at 11,500 rpm for 45 minutes in the Fann Multi-Mixer, Model 9B5 (Fann Instruments, Inc, Houston Tex.). Three drops of Bara Defoam (NL Baroid/NL Industries, Inc., Houston, Tex.) was added and stirring was continued for an additional 30 seconds. The mixing cup was removed from the mixer and immersed in chilled water to lower the fluid's temperature, then placed in a constant temperature bath at 25° C. The solution was transferred to a 400-ml tall form beaker.

Fann viscosity (Fann Viscometer, Model 35A) was measured while mixing at low speed (3 rpm). The shear stress value was read from the dial and recorded as the SWv value at 3 rpm.

The viscosity was also determined on the Brookfield LV DV-II or DV-II viscometer with the LV-2C spindle. The 0.06 sec⁻¹ reading was measured at 0.3 rpm.

EXAMPLE 12 Materials and Methods

Medium. YM contains per liter, 3 g yeast extract, 5 g peptone, 3 g malt extract, and 10 g glucose. DM2 medium contains per liter, 2.68 g K₂HPO₄, 1.31 g KH₂PO₄, 2.0 g NH₄SO₄, 0.1 g MgSO₄.7H₂O, 15 mg CaCl₂.2H₂O, 8.34 mg FeSO₄.7H₂O, 0.05 mg MnCl₂.4H₂O, 0.03 mg CoCl₂.6H₂O, 0.8 mg CuSO₄.5H₂O, 0.02 mg Na₂MoO₄.2H₂O, 1.0 mg ZnSO₄.7H₂O, 0.2 mg H₃BO₃ and 10 g glucose. Gellan shake flask fermentation medium contains per liter, 0.23 g NaCl, 0.165 g CaCl₂.2H₂O, 2.8 g K₂HPO₄, 1.2 g KH₂PO₄, 1.9 g NaNO₃, 1.0 g N-Z-Amine type EKC (Sheffield Products), 36.46 g Star-Dri corn syrup, 2.5 mg FeSO₄.7H₂O, 24 μg CoCl₂.6H₂O and 0.1 g MgSO₄.7H₂O.

Centrifugation test for slime. Strains were grown approximately 24 hours at 30° C. in DM2 medium containing 1% glucose, with shaking at 350 rpm and then centrifuged at maximum speed (10,000 rpm) for 5 minutes in the Eppendorf centrifuge.

Hot settling test. Strains were grown in gellan shake flask fermentation medium. Fermentation broth was heated in the autoclave for 10 minutes to liquefy gellan. The hot broth was then transferred to a large test tube and allowed to settle overnight at 95° C. (to maintain broth as liquid). With a capsular strain the cells are attached to the polysaccharide and remain suspended. For slime-formers, the cells are not attached and precipitate during overnight incubation.

PCR amplification. We used the high fidelity PCR enzyme “PfuUltra hot start DNA polymerase” from Stratagene (LaJolla, Calif.).

REFERENCES

The disclosure of each reference cited is expressly incorporated herein.

-   1. Coleman R C. 2001. Cloning and analysis of Sphingomonas sp. ATCC     53159 polysaccharide genes. San Diego State University MS thesis -   2. Ditta G, S Stanfield, D Corbin and D R Helinski. 1980. Broad host     range DNA cloning system for Gram-negative bacteria: construction of     a gene bank of Rhizobium meliloti. Proc Natl Acad Sci USA 77:     7347-7351. -   3. Harding N E, Y N Patel and R J Coleman. 2004. Organization of     genes required for gellan polysaccharide biosynthesis in     Sphingomonas elodea ATCC 31461. J Ind Microbiol Biotechnol 31:70-82. -   4. Lenz, O., E. Schwartz, J. Demedde, M. Eitinger and B.     Friedrich. 1994. The Alcaligenes eutrophus H116 hoxX gene     participates in hydrogenase regulation. J. Bacteriol. 176:4385-4393. -   5. Matthews T D. 2004. Identification of genes involved in     phenotypic phase shifting of Sphingomonas sp. ATCC 53159 San Diego     State University MS thesis -   6. Pollock T J and R W Armentrout. 1999. Planktonic/sessile     dimorphism of polysaccharide-encapsulated Sphingomonads. J Ind     Microbiol Biotechnol 23: 436-441. -   7. Pollock, T J, W A T van Workum, L Thome, M Mikolajczak, M     Yamazaki, J W Kijne and R W Armentrout. 1998. Assignment of     biochemical functions to glycosyl transferase genes which are     essential for biosynthesis of exopolysaccharides in Sphingomonas     strain S88 and Rhizobium leguminosarum. J Bacteriol 180: 586-593. -   8. Sa-Correia I, A M Fialho, P Videira, L M Moreira, A R Marques and     H Albano. 2002. Gellan gum biosynthesis in Sphingomonas paucimobilis     ATCC 31461: Genes, enzymes and exopolysaccharide production     engineering. J Ind Microbiol Biotechnol. 29: 170-176. -   9. Yamazaki M, L Thome, M Mikolajczak, R W Armentrout and T J     Pollock. 1996. Linkage of genes essential for synthesis of a     polysaccharide capsule in Sphingomonas strain S88. J Bacteriol 178:     2676-2687. -   10. Yamazaki M, M Mikolajczak, T J Pollock and R W Armentrout. 2003.     Production of exopolysaccharides unattached to the surface of     bacterial cells. U.S. Pat. No. 6,605,461. -   11. Cleary, Joseph M., et al. Genetically purified gellan gum. U.S.     Patent Application No. 20060003051. 

1. A method of making a bacterium of the genus Sphingomonas which comprises a mutation in one or both genes selected from the group consisting of genes M and N of the sphingan polysaccharide biosynthetic gene cluster, comprising: isolating a segment of genomic DNA of a first bacterium of the genus Sphingomonas, wherein the segment comprises all or part of genes M and/or N of the sphingan polysaccharide biosynthetic gene cluster; inducing a mutation in the segment to form a mutated segment; introducing the mutated segment into a second bacterium of the genus Sphingomonas, wherein the second bacterium comprises wild-type genes M and/or N of the sphingan polysaccharide biosynthetic gene cluster; isolating a progeny of the second bacterium in which the mutated segment has integrated in the genome and replaced wild-type genes M and/or N of the sphingan polysaccharide biosynthetic gene cluster of the second bacterium.
 2. A method of making a bacterium of the genus Sphingomonas which comprises a mutation in one or both genes selected from the group consisting of genes M and N of the sphingan polysaccharide biosynthetic gene cluster, comprising: isolating two non-contiguous segments of genomic DNA of a first bacterium of the genus Sphingomonas, wherein the segments flank or include genes M and N of the sphingan polysaccharide biosynthetic gene cluster; ligating the two non-contiguous segments together; introducing the ligated non-contiguous segments into a second bacterium of the genus Sphingomonas, wherein the second bacterium comprises wild-type genes M and/or N of the sphingan polysaccharide biosynthetic gene cluster; isolating a progeny of the second bacterium in which the ligated segment has integrated in the genome and replaced wild-type genes M and/or N of the sphingan polysaccharide biosynthetic gene cluster of the second bacterium.
 3. The method of claim 1 wherein the segment of genomic DNA is isolated by amplification.
 4. The method of claim 1 wherein the segment of genomic DNA is isolated by synthesis.
 5. The method of claim 1 wherein the segment of genomic DNA is isolated by purification from genomic DNA.
 6. The method of claim 2 wherein the segments of genomic DNA are isolated by amplification.
 7. The method of claim 2 wherein the segments of genomic DNA are isolated by synthesis.
 8. The method of claim 2 wherein the segments of genomic DNA are isolated by purification from genomic DNA.
 9. A composition comprising a diutan polysaccharide which imparts to a fluid an increased viscosity relative to an equivalent amount of diutan produced by strain ATCC
 53159. 10. The composition of claim 9 wherein the increased viscosity is at least 30% more than strain ATCC
 53159. 11. The composition of claim 9 wherein the increased viscosity is at least 40% more than strain ATCC
 53159. 12. The composition of claim 9 wherein the increased viscosity is at least 50% more than strain ATCC
 53159. 13. The composition of claim 9 wherein the increased viscosity is at least 60% more than strain ATCC
 53159. 14. The composition of claim 9 wherein the increased viscosity is at least 70% more than strain ATCC
 53159. 15. The composition of claim 9 wherein the increased viscosity is at least 80% more than strain ATCC
 53159. 16. The composition of claim 9 wherein the increased viscosity is at least 90% more than strain ATCC
 53159. 17. An isolated and purified bacterium of the genus Sphingomonas which comprises a deletion in one or both genes selected from the group consisting of genes M and N of the sphingan polysaccharide biosynthetic gene cluster.
 18. The bacterium of claim 17 which is of the species S. elodea.
 19. The bacterium of claim 17 which is not of the species S. elodea.
 20. The bacterium of claim 17 which is a Sphingomonas spp. of the same species as the bacterium deposited as ATCC
 53159. 21. The bacterium of claim 17 wherein the sphingan polysaccharide is diutan.
 22. The bacterium of claim 17 wherein the sphingan polysaccharide is gellan.
 23. The bacterium of claim 17 wherein the sphingan polysaccharide is not gellan.
 24. The bacterium of claim 17 wherein the sphingan polysaccharide is welan.
 25. The bacterium of claim 17 wherein the sphingan polysaccharide is rhamsan.
 26. The bacterium of claim 17 wherein the bacterium contains no exogenous DNA.
 27. The bacterium of claim 17 wherein the bacterium comprises a deletion of some or all of gelM.
 28. The bacterium of claim 17 wherein the bacterium comprises a deletion of some or all of gelN.
 29. The bacterium of claim 17 wherein the bacterium comprises a deletion of some or all of dpsM.
 30. The bacterium of claim 17 wherein the bacterium comprises a deletion of some or all of dpsN.
 31. The bacterium of claim 17 wherein the bacterium comprises a deletion of some or all of gelM and gelN.
 32. The bacterium of claim 17 wherein the bacterium comprises a deletion of some or all of dpsM and dpsN.
 33. A method of producing a sphingan polysaccharide, comprising: culturing the bacterium of claims 17 in a culture medium under conditions suitable for producing sphingan polysaccharide whereby sphingan polysaccharide is produced in the culture medium.
 34. The method of claim 33 further comprising the step of: separating the sphingan polysaccharide from bacteria in the culture medium.
 35. The method of claim 34 wherein the step of separating is performed by centrifugation.
 36. The method of claim 34 wherein the step of separating is performed by sedimentation.
 37. The method of claim 34 wherein the step of separating comprises treatment of the culture medium with alkali.
 38. The method of claim 34 wherein the step of physically separating comprises a treatment of the culture medium with enzyme.
 39. The method of claim 34 wherein the sphingan polysaccharide is diutan.
 40. The method of claim 33 wherein the sphingan polysaccharide is gellan.
 41. The method of claim 33 wherein the sphingan polysaccharide is not gellan.
 42. The method of claim 33 wherein the bacterium is a S. elodea.
 43. The method of claim 33 wherein the bacterium is not a S. elodea.
 44. The method of claim 33 wherein the bacterium is a Sphingomonas spp. of the same species as the bacterium deposited as ATCC53159.
 45. The method of claim 33 wherein the sphingan polysaccharide is welan.
 46. The method of claim 33 wherein the sphingan polysaccharide is rhamsan.
 47. The method of claim 33 wherein the bacterium comprises a deletion of some or all of gelM.
 48. The method of claim 33 wherein the bacterium comprises a deletion of some or all of gelN.
 49. The method of claim 33 wherein the bacterium comprises a deletion of some or all of dpsM.
 50. The method of claim 33 wherein the bacterium comprises a deletion of some or all of dpsN.
 51. The method of claim 33 wherein the bacterium comprises a deletion of some or all of gelM and gelN.
 52. The bacterium of claim 33 wherein the bacterium comprises a deletion of some or all of dpsM and dpsN.
 53. A culture broth comprising the bacterium of claim
 17. 54. A culture broth comprising the bacterium of claim
 18. 55. A culture broth comprising the bacterium of claim
 19. 56. A culture broth comprising the bacterium of claim
 20. 57. A culture broth comprising the bacterium of claim
 21. 58. A culture broth comprising the bacterium of claim
 22. 59. A culture broth comprising the bacterium of claim
 23. 60. A culture broth comprising the bacterium of claim
 24. 61. A culture broth comprising the bacterium of claim
 25. 62. A culture broth of claim 53 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 63. A culture broth of claim 54 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 64. A culture broth of claim 55 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 65. A culture broth of claim 56 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 66. A culture broth of claim 57 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 67. A culture broth of claim 58 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 68. A culture broth of claim 59 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 69. A culture broth of claim 60 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 70. A culture broth of claim 61 wherein the culture broth has been subjected to a procedure to remove the bacterium from the culture broth.
 71. A method of making a bacterium of the genus Sphingomonas which comprises a mutation in gene I of the sphingan polysaccharide biosynthetic gene cluster, comprising: isolating a segment of genomic DNA of a first bacterium of the genus Sphingomonas, wherein the segment comprises all or part of gene I of the sphingan polysaccharide biosynthetic gene cluster; inducing a mutation in the segment to form a mutated segment; introducing the mutated segment into a second bacterium of the genus Sphingomonas, wherein the second bacterium comprises wild-type genes I of the sphingan polysaccharide biosynthetic gene cluster; isolating a progeny of the second bacterium in which the mutated segment has integrated in the genome and replaced wild-type gene I of the sphingan polysaccharide biosynthetic gene cluster of the second bacterium.
 72. A method of making a bacterium of the genus Sphingomonas which comprises a mutation in gene I of the sphingan polysaccharide biosynthetic gene cluster, comprising: isolating a segment of genomic DNA of a first bacterium of the genus Sphingomonas, wherein the segments flanks or includes gene I of the sphingan polysaccharide biosynthetic gene cluster; introducing the segment into a second bacterium of the genus Sphingomonas, wherein the second bacterium comprises wild-type gene I of the sphingan polysaccharide biosynthetic gene cluster; isolating a progeny of the second bacterium in which the segment has integrated in the genome and replaced wild-type genes I of the sphingan polysaccharide biosynthetic gene cluster of the second bacterium.
 73. The method of claim 71 wherein the segment of genomic DNA is isolated by amplification.
 74. The method of claim 71 wherein the segment of genomic DNA is isolated by synthesis.
 75. The method of claim 71 wherein the segment of genomic DNA is isolated by purification from genomic DNA.
 76. The method of claim 72 wherein the segments of genomic DNA are isolated by amplification.
 77. The method of claim 72 wherein the segments of genomic DNA are isolated by synthesis.
 78. The method of claim 72 wherein the segments of genomic DNA are isolated by purification from genomic DNA.
 79. A method of making a bacterium of the genus Sphingomonas which comprises a mutation in gene R of the sphingan polysaccharide biosynthetic gene cluster, comprising: isolating a segment of genomic DNA of a first bacterium of the genus Sphingomonas, wherein the segment comprises all or part of gene R of the sphingan polysaccharide biosynthetic gene cluster; inducing a mutation in the segment to form a mutated segment; introducing the mutated segment into a second bacterium of the genus Sphingomonas, wherein the second bacterium comprises wild-type genes R of the sphingan polysaccharide biosynthetic gene cluster; isolating a progeny of the second bacterium in which the mutated segment has integrated in the genome and replaced wild-type gene R of the sphingan polysaccharide biosynthetic gene cluster of the second bacterium.
 80. A method of making a bacterium of the genus Sphingomonas which comprises a mutation in one or both genes selected from the group consisting of gene R of the sphingan polysaccharide biosynthetic gene cluster, comprising: isolating a segment of genomic DNA of a first bacterium of the genus Sphingomonas, wherein the segment flanks or include gene R of the sphingan polysaccharide biosynthetic gene cluster; introducing the segment into a second bacterium of the genus Sphingomonas, wherein the second bacterium comprises wild-type gene R of the sphingan polysaccharide biosynthetic gene cluster; isolating a progeny of the second bacterium in which the segment has integrated in the genome and replaced wild-type gene R of the sphingan polysaccharide biosynthetic gene cluster of the second bacterium.
 81. The method of claim 79 wherein the segment of genomic DNA is isolated by amplification.
 82. The method of claim 79 wherein the segment of genomic DNA is isolated by synthesis.
 83. The method of claim 79 wherein the segment of genomic DNA is isolated by purification from genomic DNA.
 84. The method of claim 80 wherein the segments of genomic DNA are isolated by amplification.
 85. The method of claim 80 wherein the segments of genomic DNA are isolated by synthesis.
 86. The method of claim 80 wherein the segments of genomic DNA are isolated by purification from genomic DNA. 